Canonical Allele Identifier: CA2082777948

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32316923_32316924delinsCG , CM000675.2:g.32316923_32316924delinsCG	GRCh38
NC_000013.10:g.32891060_32891061delinsCG , CM000675.1:g.32891060_32891061delinsCG	GRCh37
NC_000013.9:g.31789060_31789061delinsCG	NCBI36
NG_012772.3:g.6444_6445delinsCG , LRG_293:g.6444_6445delinsCG
NG_017006.1:g.31_32delinsCG
NG_017006.2:g.3440_3441delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.67+396_67+397delinsCG	ENSP00000434898.2:n.67+396_67+397delinsCG
ENST00000528762.2:c.67+396_67+397delinsCG	ENSP00000433168.2:n.67+396_67+397delinsCG
ENST00000530893.7:c.-303+400_-303+401delinsCG	ENSP00000499438.2:n.-303+400_-303+401delinsCG
ENST00000665585.2:c.67+396_67+397delinsCG	ENSP00000499570.2:n.67+396_67+397delinsCG
ENST00000666593.2:c.67+396_67+397delinsCG	ENSP00000499256.2:n.67+396_67+397delinsCG
ENST00000700202.2:c.67+396_67+397delinsCG	ENSP00000514856.2:n.67+396_67+397delinsCG
ENST00000700200.1:n.191+396_191+397delinsCG
ENST00000700201.1:c.67+396_67+397delinsCG	ENSP00000514855.1:n.67+396_67+397delinsCG
ENST00000380152.8:c.67+396_67+397delinsCG MANE Select	ENSP00000369497.3:n.67+396_67+397delinsCG
ENST00000544455.6:c.67+396_67+397delinsCG	ENSP00000439902.1:n.67+396_67+397delinsCG
ENST00000614259.2:c.67+396_67+397delinsCG	ENSP00000506251.1:n.67+396_67+397delinsCG
ENST00000680887.1:c.67+396_67+397delinsCG	ENSP00000505508.1:n.67+396_67+397delinsCG
ENST00000380152.7:c.67+396_67+397delinsCG	ENSP00000369497.3:n.67+396_67+397delinsCG
ENST00000530893.6:n.265+400_265+401delinsCG
ENST00000544455.5:c.67+396_67+397delinsCG	ENSP00000439902.1:n.67+396_67+397delinsCG
ENST00000614259.1:n.67+396_67+397delinsCG
NM_000059.3:c.67+396_67+397delinsCG , LRG_293t1:c.67+396_67+397delinsCG	NP_000050.2:n.67+396_67+397delinsCG
XM_011535203.1:c.67+396_67+397delinsCG	XP_011533505.1:n.67+396_67+397delinsCG
XM_011535204.1:c.67+396_67+397delinsCG	XP_011533506.1:n.67+396_67+397delinsCG
XM_011535205.1:c.67+396_67+397delinsCG	XP_011533507.1:n.67+396_67+397delinsCG
NM_000059.4:c.67+396_67+397delinsCG MANE Select	NP_000050.3:n.67+396_67+397delinsCG